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Boli A-Z 3-Methylglutaconic Aciduria 3-Methylglutaconic Aciduria, Type I 3-Methylglutaconic Aciduria, Type Iii 3-Methylglutaconic Aciduria, Type Iv 3-Methylglutaconic Aciduria, Type Ix 3-Methylglutaconic Aciduria, Type Viii 3-Methylglutaconic Aciduria with Deafness, Encephalopathy, and Leigh-Like Syndrome Aceruloplasminemia Adie Pupil Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Al-Raqad Syndrome Aniridia 1 Anorexia Nervosa 1 Apraxia Arthrochalasia Ehlers-Danlos Syndrome Ataxia and Polyneuropathy, Adult-Onset Ataxia-Oculomotor Apraxia 3 Atrial Standstill 1 Autosomal Dominant Progressive External Ophthalmoplegia Barth Syndrome Blood Group--Ahonen Chronic Progressive External Ophthalmoplegia Cortical Blindness Diabetic Polyneuropathy Diffuse Cutaneous Mastocytosis Dilated Cardiomyopathy Encephalomyopathy Hepatic Adenomas, Familial Hepatitis Hypospadias Kearns-Sayre Syndrome Left Ventricular Noncompaction Long Qt Syndrome Microcytic Anemia Mitochondrial Dna-Associated Leigh Syndrome and Narp Mitochondrial Dna Depletion Syndrome 1 Mitochondrial Dna Depletion Syndrome 4a Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes Mitochondrial Neurogastrointestinal Encephalomyopathy Mitochondrial Neurogastrointestinal Encephalopathy Disease Myoclonic Epilepsy Associated with Ragged-Red Fibers Neonatal Period Electroclinical Syndrome Ocular Motility Disease Optic Atrophy 3, Autosomal Dominant Organic Acidemia Paralytic Ileus Scotoma Sensory Ataxic Neuropathy, Dysarthria, and Ophthalmoparesis Tritanopia